Details
| Original language | English |
|---|---|
| Pages (from-to) | 419-421 |
| Number of pages | 3 |
| Journal | Journal of the Chemical Society, Perkin Transactions 1 |
| Issue number | 2 |
| Publication status | Published - 1990 |
| Externally published | Yes |
Abstract
The reaction of epoxysilanes with lithiated allylsilanes gives predominantly α-silyl-substituted alcohols (3) which are convenient precursors for the preparation of 1-silyl-substituted 1,4-dienes.
ASJC Scopus subject areas
- Chemistry(all)
- General Chemistry
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In: Journal of the Chemical Society, Perkin Transactions 1, No. 2, 1990, p. 419-421.
Research output: Contribution to journal › Article › Research › peer review
}
TY - JOUR
T1 - Regiospecific synthesis of 1-silyl substituted 1,4-dienes
AU - Schaumann, Ernst
AU - Kirschning, Andreas
PY - 1990
Y1 - 1990
N2 - The reaction of epoxysilanes with lithiated allylsilanes gives predominantly α-silyl-substituted alcohols (3) which are convenient precursors for the preparation of 1-silyl-substituted 1,4-dienes.
AB - The reaction of epoxysilanes with lithiated allylsilanes gives predominantly α-silyl-substituted alcohols (3) which are convenient precursors for the preparation of 1-silyl-substituted 1,4-dienes.
UR - http://www.scopus.com/inward/record.url?scp=37049077583&partnerID=8YFLogxK
U2 - 10.1039/p19900000419
DO - 10.1039/p19900000419
M3 - Article
AN - SCOPUS:37049077583
SP - 419
EP - 421
JO - Journal of the Chemical Society, Perkin Transactions 1
JF - Journal of the Chemical Society, Perkin Transactions 1
SN - 1472-7781
IS - 2
ER -